Objective This study aimed to determine the prevalence and associated factors of poor sleep quality among pregnant women in Ethiopia.
Method Institutional based cross-sectional study.
Setting University of Gondar Comprehensive Specialized Hospital, Gondar, Ethiopia.
Participants A total of 415 pregnant women were recruited by using a systematic random sampling technique from 28 April 2020 to 12 June 2020.
Measurement The desired data were collected through face-to-face interview technique by using validated questionnaires such as the Pittsburgh Sleep Quality Index, Edinburgh Postnatal Depression Scale, Perceived Stress Scale, Oslo-3 and Abuse Assessment Screen. The data were analysed by using SPSS V.20. Logistic regression analysis was used to identify associated factors with poor sleep quality. Variables having a p value of less than 0.2 in the bivariate analysis were entered to the multivariable logistic regression. A p value of less than 0.05 was considered statistically significant, at 95% CI.
Result In this study, 175 (42.2%) pregnant women had poor sleep quality. According to multivariable logistic regression, being first and third trimesters of gestational age (adjusted OR (aOR) 2.31, 95% CI 1.16 to 4.61 and aOR 3.45, 95% CI 2.05 to 5.79, respectively), consumption of caffeinated substances (aOR 2.96, 95% CI 1.68 to 5.52), having depression (aOR 2.12, 95% CI 1.19 to 3.76), having high perceived stress (aOR 5.39, 95% CI 1.96 to 14.79) and experience of intimate partner violence (aOR 5.57, 95% CI 2.19 to 14.68) were positive significant associated factors with poor sleep quality.
Conclusion and recommendation The prevalence of poor sleep quality among pregnant women was relatively high. First and third trimesters, consumption of caffeinated substances, antenatal depression, high perceived stress and intimate partner violence were factors significantly associated with poor sleep quality. This result suggests that all pregnant women should be screened and treated for poor sleep quality during the first and third trimesters.
- sleep medicine
- maternal medicine
- mental health
- reproductive medicine
Data availability statement
The dataset is available on request by emailing the corresponding author (email@example.com).
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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Strengths and limitations of this study
The Pittsburgh Sleep Quality Index, which is validated and has high sensitivity and specificity, has been used to assess the outcome variable of sleep quality among pregnant women.
Due to the nature of cross-sectional study design, it could not report the temporal cause-and-effect relationship between depression and poor sleep quality.
Individuals who had no symptoms of sleep problem may have less motivation to recall earlier exposure than individuals with the symptoms.
Sleep is a basic requisite for human physiological and psychological functioning.1 2 It is a complex physiological process to restore energy, physical ability to think and the ability to understand quickly.3 It is a systematic and organised behaviour that is regularly repeated on the basis of a biological rhythm. Sleep significantly contributes to the restoration or renewal of mental and physiological power and is required for doing new tasks and responsibilities.4
Sleep is essential for the normal growth and development of both mind and body. A good sleep pattern is important for a healthy pregnancy. During pregnancy, there is a need to get adequate sleep for the normal growth and development of the fetus.5 During pregnancy, getting appropriate sleep gives the mother the energy that they need for their delivery process.1 2
Sleep disorders such as insomnia are common during pregnancy.6 Despite being a natural phenomenon, pregnancy is associated with major hormonal, psychological and physiological changes. Previous studies showed that more than two-thirds of women experience changes in sleep during pregnancy.7 This sleep problem in general worsens with every subsequent trimester.3 One in four women experiences sleep problems in the first trimester of pregnancy, and this increases to three in four women in the third trimester.8 9
Sleep problem is a common problem for pregnant women, in which more than four out of five pregnant women are affected by sleep disturbances. Furthermore, depressive symptoms, increased age and gestational age were found to be factors leading to poor sleep quality in pregnant women.10
Previous studies showed that pregnant women with poor quality of sleep had a 20% increased chance of undergoing caesarean section and prolonged labour.11 Poor sleep quality has been shown to be a prospective risk factor for depression both during the prenatal and postpartum period.12–14 African-American pregnant women with poor sleep quality had 10.2 times increased risks of preterm birth compared with those with good sleep quality.15
The quantity and quality of sleep during pregnancy have been shown to be altered.16 Some previous studies have documented trimester-specific changes in sleep architecture. Different literature also indicate that sleep disturbances during pregnancy are associated with women’s poor health outcomes like intrauterine growth restriction, preterm birth, stillbirth, and low Appearance, Pulse, Grimacing, Activity and Respiration (Apgar) score on the newborn.5 17 18 Poor sleep quality has also been indicated to have maternal complications during pregnancy period like pre-eclampsia, gestational diabetes as well as increased complications during delivery like prolonged labour and caesarean section.13 17
Sleep disturbances among pregnancies reported that sleep deprivation might increase the risk of mental disorders that ranges from postpartum depression to overt psychosis and also increases the possibility of accidents.19 Although several studies have assessed sleep quality during pregnancy and its associated factor, most of these studies were conducted in the western population or developed countries.
Despite the high prevalence and multiple complications of poor sleep quality among pregnant women, it is under-recognised and largely undermined by caregivers (clinicians) as well as the government. The extent of poor sleep quality and its associated factors among pregnant women is not well known in low-and-middle-income countries including Ethiopia. To the best of the investigators’ knowledge, there is no published study on the prevalence of poor sleep quality and its associated factor during pregnancy among the Ethiopian pregnant. Therefore, this study aimed to determine the magnitude of poor sleep quality and associated factors among pregnant women attending the antenatal care (ANC) units at University of Gondar Comprehensive Specialized Hospital (UoGCSH), with the aim of instituting appropriate intervention programmes.
Methods and materials
Study design and study period
An institutional-based cross-sectional study was conducted to assess the prevalence and associated factors of poor sleep quality among pregnant women at UoGCSH Antenatal Care Clinic from 28 April to 12 June 2020.
This study was conducted at UoGCSH, ANC clinic, Gondar, Amhara, Northwest Ethiopia. ANC service in the hospital has been given by obstetricians and gynaecologists and midwives in the outpatient departments. Approximately 11 000 pregnant women per year have been taking ANC service per year.
We have included all pregnant women ≥18 years of age attending ANC clinic at UoGCSH.
Severely ill pregnant women (bleeding, hyperemesis) were excluded from this study, as were women in labour and those who had difficulty communicating for interview during the data collection period.
Sample size determination
We applied a single proportion formula to calculate the required sample size. On sample size calculation, the following considerations were taken; margin of error (d) 5%, level of confidence (95%), proportion (p) 50% (as there was no previously published study conducted in Ethiopia) and adding 10% non-response rate. Therefore, the final sample size was taken to 423.
Sampling technique and procedure
We engaged in systematic sampling of every other woman who attended ANC during the 28 April to 12 June 2020 time frame.
Data collection tool and procedure
Data were collected from study subjects using validated and pre-tested structured questionnaires. The data were collected by four BSc psychiatry professionals after 1-day training had been given and facilitated by the principal investigator.
The interview structure consists of eight parts.
Demographic data which gave baseline information were obtained from the participants including age, ethnicity, religion, education, occupation, marital status and residency.
Obstetrics and gynaecological characteristics
Gynaecological, obstetrical and associated clinical factors giving information such as gestational age, parity, gravidity, the experience of abortion, type of pregnancy and other comorbid illnesses like pregnancy-related hypertension, gestational diabetes mellitus and other illness were obtained from the participants and from their medical records.
The Pittsburgh Sleep Quality Index (PSQI) is a 19-item self-reported questionnaire that evaluates sleep quality over the past month. The PSQI gives seven sleep components to assess sleep quality including subjective sleep quality, duration of sleep, sleep disturbance, sleep latency, habitual sleep efficiency, use of sleep medication and daytime dysfunction.20 Each sleep component gives a score ranging from 0 to 3, with 3 indicating the more severe problem. The sleep component scores are added to obtain a global sleep quality score that ranges from 0 to 21. Higher scores indicate poor sleep quality during the previous month. Participants with a global score of greater than 5 were classified as poor sleepers.21 The PSQI is validated in Ethiopia for community-dwelling Ethiopian adults with Cronbach’s α of 0.73.22 23 Higher scores indicate poorer sleep quality. A global score of greater than 5 yielded a diagnostic sensitivity of 90% and specificity of 87% in distinguishing good and poor sleepers with a Cronbach’s α of 0 .73 in pregnant women24 and a Cronbach’s α of this study was 0.71.25
Behavioural factors including use of alcohol, use of tobacco, khat chewing and consumption of caffeinated substance were assessed by using structured questionnaires adapted from WHO ASSIST V.3.26 Participants who used substances like tobacco, khat and alcohol only for non-medical purposes during their lifetime were considered as ever substance users and pregnant women who used substances like tobacco, khat and alcohol only for non-medical purposes during the last 3 months are considered as current substance users.26
Use of caffeinated substance
If positive for consumption of one or more of the substances coffee, tea and Coca-Cola during the last 1 month.
Clinical related characteristics
Antenatal depression was assessed with the Edinburgh Postnatal Depression Scale (EPDS) which consists of 10 items. EPDS has been used successfully across diverse cultural settings. The EPDS questionnaire has been validated as effective in measuring prenatal depression.24 Items are rated on a 4-point scale from 0 (not at all) to 3 (yes, most of the time). Total scores range from 0 to 30. The screening tool has been validated for detecting depression in antepartum and postpartum samples in many countries. The instrument was validated in public health centres in Addis Ababa for post partum and showed a sensitivity of 84.6% and specificity of 77.0% at the cut-off score 7/8 and Cronbach’s α of 0.71.24 The cut-off point of EPDS among pregnant women is usually higher than postpartum women.27 Like other studies conducted globally and in Ethiopia, in this study, a cut-off point of 13 was used to identify pregnant women with depressive symptoms.28–30 Those pregnant women who scored 13 and above were categorised as having depression while pregnant scored below 13 were non-depressed28 and a Cronbach’s α of this study was 0.74.
Social support related characteristics
A three-item questionnaire was used to determine the status of social support, which was assessed by using Oslo-3 validated tool. Oslo 3-item Social Support Scale has the sum score scale ranging from 3 to 14 with three broad categories: ‘poor social support’ 3–8, ‘moderate social support’ 9–11 and ‘strong social support’ 12–14 (with Cronbach’s α=0.88, 86% sensitivity and 67% specificity).30
Perceived stress characteristics
Perceived stress resulting from perceptions of difficulty in control or ability to cope with life events during the last 1 month was measured by the 10-item Perceived Stress Scale (PSS).31 Responses are rated on a 5-point scale from 0 (never) to 4 (very often). Some of the PSS scores are obtained by reversing responses (eg, 0=4, 1=3, 2=2, 3=1 and 4=0) to the four positively stated items (items 4, 5, 7 and 8) and then summed across all scale items. Scores range from 0 to 40, with higher scores indicating perceived higher stress. The Cronbach’s alpha for this instrument is between 0.84 and 0.86,31 and the Cronbach’s α of this study was 0.89.
Intimate partner violence characteristics
Consisted of five questions to determine the status of intimate partner violence. The questionnaire was developed from WHO Multi-Country Study on Violence Against Women, and if any questions on the screen were answered yes, the participant is considered positive for abuse.32
Data quality control
Data were collected using face-to-face structured interviews. The study subjects were informed about the general information regarding the study objectives as well as the opportunities or benefits that this study could bring. Finally, the filled questionnaires were checked for consistency and completeness daily. To assure the data quality, high emphasis was given in designing data collection instruments. The questionnaire was prepared in English and translated to Amharic and back to English to maintain consistency. The Amharic version questionnaires were used to collect information. One-day training was given for data collectors and supervisors by the principal investigator on the methods of data collection. The questionnaire was pretested 1 week before the actual data collection on 5% of the total same size that were not included in the main survey.
Data processing and analysis
Data were coded and entered using Epidata software V.126.96.36.199, and then were exported and analysed by using SPSS V.20. Questionnaires that were incomplete were considered as non-response (n=8). The data were analysed to generate descriptive statistics—means, medians, frequency, percentages and SD—using SPSS V.20. The goodness of fit was checked by Hosmer and Lemeshow (p=0.52). Multicollinearity (the values of Variance Inflation Factor (VIF) were <1.08) and χ2 assumptions were done. Logistic regression analysis was used to calculate adjusted ORs (aORs) to control for confounding variables with a 95% CI. Variables with p value less than 0.2 in bivariate logistic regression analysis were entered into multivariable logistic regression to detect if there is a significant association. Outcome and independent variables were entered into bivariate one by one to detect association and to multivariable logistic regression to show the presence and strength of association. Statistical significance was determined at p value <0.05.
Patient and public involvement
In this study, participants were pregnant women who were attending ANC at UoGCSH. Seriously sick patients were excluded. We did not involve participants in designing the study and the recruitment process. The result of this study has been submitted to the Department of Psychiatry, University of Gondar, and UoGCSH.
Sociodemographic characteristics of the participants
In total, 415 pregnant women participated in the study with a response rate of 98.1%. The mean age of the participants was 28 years (SD±5.4); 225 (54.2%) were within the range of 26–35 years. Three hundred ninety-one (94.2%) were married and 302 (72.8%) were Orthodox by religion; 156 (37.6%) of the participants had primary education and 118 (28.4%) had a diploma and above; 406 (97.8%) of the study population were Amhara in ethnicity and 168 (40.5%) were housewives in occupation; 391 (94.2%) of the participants were living in urban areas (table 1).
Characteristics of gynaecological, obstetrical and other comorbid illnesses
In total, 196 (47.2%) of the participants were in the third trimester and nearly one-third (123, 29.6%) were experiencing their first pregnancy; 149 (35.9%) had an experience of labour two or more times before and 133 (32%) of the participants had two or more children alive; 62 (14.9%) had experienced an abortion in their lifetime and 356 (88.7%) were wanted pregnancy in current pregnancy; 58 (14%) of the participants had other comorbid illnesses, and of those, 37 (63%) and 16 (27.6%) had pregnancy-related hypertension/pre-eclampsia and gestational diabetes mellitus, respectively.
Prevalence of poor sleep quality among pregnant women
The average time to go to bed at night was 21:37 and the average time to rise was 12:22. The average sleeping duration was 7.43 hours with SD±1.59.
The prevalence of poor sleep quality among the participants was 42.2% (95% CI 37.4% to 47.6%) with proportion of 45.9%, 26.6% and 53.6% in their first, second and third trimesters, respectively. The median PSQI score of the participants was 5.00 with a range of 0–17. Eighteen (4.3%) had very bad subjective sleep quality; 162 (39.0%) had sleep latency that took 31–60 min, and with regard to sleep duration, 221 (53.3%) had actual sleep per night of more than 7 hours; 268 (64.5%) of the participants had more than 85% sleep efficiency, while the median of sleep disturbance was 7.0 (IQR 5–9); 401 (96.6%) of the study population did not use sleep medication during the last 1 month (table 2).
Behavioural characteristics of the participants
In total, 411 (99%) of the participants had not ever smoked tobacco in their lifetime and there were no participants who smoked tobacco in the last 3 months. Forty-eight (11.6%) of the study participants had used alcohol in their lifetime and 26 (6.3%) used alcohol within the last 3 months. Among those pregnant women who had used alcohol during the last 3 months, 14 (53.8%) used tella (local alcoholic beverage). Five (1.2%) of the participants had ever chewed khat, but there was no one reporting using khat in the last 3 months. Also, 310 (74.7%) of the participants used a caffeinated substance for the last 1 month, and from those, 209 (67.7%) and 45 (14.5%) used coffee and both coffee and tea on a daily basis; 206 (80.2%) consumed two or more cups of coffee per day.
Mental illness and psychosocial factors
Of the study participants, 86 (20.7%) had antenatal depression and 29 (7.0%) had high and 83 (20.0%) moderate perceived stress. Also, 103 (24.8%) had poor and 125 (30.1%) had strong social support.
The overall prevalence of intimate partner violence (IPV) among the participants was 29 (7.0%). Twenty participants (4.8%) had been abused physically or emotionally during their lifetime; 13 (3.1%) had been slapped, kicked or otherwise physically hurt by someone during the past 1 year, and of those, 8 (61.5%) were abused by their husbands. Eleven (2.7%) of the participants had been hit, slapped, kicked or otherwise physically hurt by someone during the current pregnancy, and of those, 8 (72.7%) were abused by their husband. Ten (2.4%) of the study participants had forced sexual activities within the past year.
Prevalence and associated factors of poor sleep quality
Prevalence of poor sleep quality
The overall prevalence of poor sleep quality among the participants attending the ANC clinic at UoGCSH was 42.2% (95% CI 37.4% to 47.6%).
Associated factors of poor sleep quality
Maternal age, educational level, gestational age, experience of abortion, consumption of caffeinated substances, antenatal depression, social support, perceived stress and IPV were variables which had a p value less than 0.2 at bivariate logistic regression. First and third trimesters of pregnancy, use of caffeinated substances, depression, high perceived stress and experience of IPV were found to be significantly associated with poor sleep quality among pregnant in multivariable logistic regression analysis at a p value of less than 0.05.
The odds of having poor sleep quality among pregnant women were 2.3 times higher in the first trimester (aOR 2.316, 95% CI 1.162 to 4.617) and 3.4 times higher in the third trimester (aOR 3.451, 95% CI 2.055 to 5.794) when compared with those in the second trimester. We took second trimester as a reference by considering the lower occurrence of poor sleep quality among those who were in their second trimester, which is supported by previous literatures.5 33 Pregnant women who consumed caffeinated substances were nearly three times likely to report poor sleep quality than non-consumers (aOR 2.964, 95% CI 1.684 to 5.215). The likelihood ratio for developing poor sleep quality among pregnant women with depression was 2.1 times that of pregnant women without depression (aOR 2.124, 95% CI 1.197 to 3.769).
The odds of having poor quality of sleep among pregnant women with high perceived stress was 5.4 times more likely compared with those with low perceived stress (aOR 5.392, 95% CI 1.965 to 14.797). The odds of having poor sleep quality among pregnant women who had experienced IPV was 5.6 times as likely when compared with pregnant women who had not experienced IPV (aOR 5.570, 95% CI 2.190 to 14.683) (table 3).
This study has found a significant number of poor sleep quality among pregnant women. Overall, this study has shown that almost one in two pregnant women experiences poor sleep quality. Different variables like pregnancy trimester, consumption of caffeinated substances, antenatal depression, high perceived stress and IPV were variables found to have a significant association with poor sleep quality.
The prevalence of poor sleep quality among pregnant women attending ANC clinics at UoGCSH was in line with studies conducted in Northwestern University (40%), Vietnam (41.2%), Iran (43.8%) and a meta-analysis study conducted globally (45.7%).11 34–36
However, this study showed higher prevalence rates of poor sleep than studies conducted in Taiwan (24.4%),37 Finland (16%)38 and Turkey (31.5%).18 Possible reasons for this discrepancy might be the characteristics of the participants, sampling techniques and the use of different measurement tools other than PSQI. Some of these studies exclude pregnant women prescribed psychiatric medication and sleeping pills or those who had chronic health problems, and night shift workers. These factors might have negative effects on sleep quality as supported by studies conducted in Rotterdam.39
The prevalence of poor sleep in this study was lower than that of studies conducted in the USA (76%),35 China (87%)10 and Taiwan (60%–65.5%).24 36 40 The possible reasons for this variation might be characteristics of the participants such as low prevalence of high perceived stress and prenatal depression among the participants of this study as compared with others,24 40 convenient sampling technique40 and internet-based data collection methods33 that might contribute to this discrepancy.
Factors like the first and third trimesters of pregnancy, consumption of caffeinated substances, antenatal depression, high perceived stress and IPV were found to be significantly associated with poor sleep quality.
First and third trimester pregnancy terms were seen as contributing factors for poor sleep quality. Respondents who were in first trimester and third trimester had the odds of having poor sleep quality more than two and three times, respectively, as compared with pregnant women in the second trimester. This study was supported by studies done in Iran33 and south India5 for both first and third trimesters, and studies conducted in China,10 Taiwan,40 USA35 and a meta-analysis study done globally36 for third trimester. The possible reasons might be increased rate of nocturnal urinary frequency, heartburn or pyrosis, daytime sleepiness, feeling of fatigue, and frequent nausea and vomiting which occurs commonly during the first trimester of pregnancy and can interfere with the quality of sleep.41 The common reasons for poor sleep quality for pregnant women during the first trimester might be a mix of excitement and surprises. The rise of progesterone levels may also be one of the reasons for poor sleep quality during the first trimester due to its soporific (sleep-inducing) and thermogenic (heat-producing) effect which is secreted from placenta and causes fatigue and earlier sleep onset and also discomfort with body change (breast tenderness).41 42 The possible reasons of poor sleep quality during the third trimester might be urinary frequency, fetal movement, lower back pain, leg cramps, heartburn, fatigue and abdominal discomfort, as reported by the American sleep foundation studies conducted in Taiwan and China.18 41–44
Consumption of caffeinated substances had a significant negative (p<0.001) effect on sleep quality. The likelihood ratio of having poor sleep quality among participants who consumed caffeinated substance was nearly three times higher than non-consumers. Other studies have shown that consumption of caffeinated substances can affect sleep quality negatively, particularly when taken later in the daytime or having multiple doses/day.45 Caffeinated substances are rapidly and almost completely (99%) absorbed.46 The effect of caffeine is primarily related to its blocking effect of A1 and A2A subtypes of adenosine receptors which is an inhibitory neuromodulator in sleep–wake regulation. Caffeine-induced wakefulness depends specifically on its antagonistic effect at A2A receptor subtype.46–48
Antenatal depression was the clinical diagnosis that showed a significant association with sleep quality during pregnancy. The likelihood of having poor sleep quality among depressed pregnant women was two times higher than non-depressed participants. This finding was similar to findings in studies conducted in China,10 49 Taiwan24 and Nepal.18 A possible reason might be the fact that persistent feelings of sadness, hopelessness and disinterest in things previously enjoyed are symptoms of depression and might result in sleep disturbances.50 Depression may also be associated with physical symptoms such as headache, back pain, gastrointestinal symptoms, fatigue, sleep problems (commonly insomnia) and daytime sleepiness.41 51 52 Symptoms of poor sleep quality at night in people with depression have been described extensively in both clinical and epidemiological studies of depressed people.53 Depression influences the stress hormone, cortisol, and adrenocorticotropic hormone, which results in the alteration of sleep patterns.54
Pregnant women with high perceived stress were found to be 5.6 times more likely to have poor sleep quality compared with pregnant women with low perceived stress during the previous month. This finding is similar to studies conducted in China49 and Taiwan.24 Stress is thought to act on sleep primarily through increased cognitive and somatic arousal during the short time before the sleep period.55
The sleep quality of the pregnant women that participated in the study was strongly affected by IPV. The women who had experienced IPV were more than 5.5 as likely to have poor sleep quality as compared with those who had no experience of IPV. This finding is supported by the study conducted in Peru.56 A possible reason might be the fact that IPV, which includes physical, emotional, or psychological and sexual abuse, is a serious community challenge that affects women around the globe. Pregnant women experiencing IPV are reported to have elevated levels of mood and anxiety disorders,57 hyperarousal and chronic stress58 which in turn might lead to poor sleep quality. Victims of IPV experience an elevated risk of sleep disturbances stemming from heightened vigilance and anticipation of violence while sleeping.59 Those women who experienced IPV had a high incidence of post-traumatic stress disorders and major depression with associated poor sleep quality.59 60
Limitation of study
Even though this study revealed important findings in the under-investigated area of sleep quality of pregnant women in Ethiopia, there were some limitations that need to be considered when generalising the results. The first limitation is the possibility of under-reporting of the events, which could be related to the data collection method we employed. There might be some recall bias as a face-to-face interview method was used.
Second, due to the nature of cross-sectional study design, it is not possible to report the temporal cause-and-effect relationship between depression and poor sleep quality. Individuals who had no symptoms of sleep problem may have less motivation to recall earlier exposure than individuals with the symptoms.
Conclusion and recommendation
The prevalence of poor sleep quality among pregnant women was relatively high. The first and third trimesters, consumption of caffeinated substances, antenatal depression, high perceived stress and IPV were factors significantly associated with poor sleep quality.
This study recommends that all pregnant women should be screened and treated for poor sleep quality during the first and third trimesters. Emphasis should be given to early detection and treatment of antenatal depression. Those with high perceived stress and those who have experienced IPV are particularly likely to report poor sleep quality during pregnancy.
Data availability statement
The dataset is available on request by emailing the corresponding author (firstname.lastname@example.org).
Patient consent for publication
This study involves human participants. Ethical clearance and official letter for permission were obtained from the institutional review board (IRB) of University of Gondar with reference number 1868/02/2020, and letter of support was given by University of Gondar College of Medicine and Health Science. Then, the letters were summated to UoGCSH Department of Gynecology and Obstetrics outpatient unit. Participants gave informed consent to participate in the study before taking part. Detailed information about the study was explained to all participants before starting data collection. Written consent was obtained from each participant before starting data collection. Study participants were told that they had the right not to participate in the study. The privacy of study participants and the confidentiality of the information were kept at every stage of data processing. Pregnant participants who complained of very bad subjective sleep quality during the time of data collection were advised to visit psychiatry OPD.
The authors would like to acknowledge the University of Gondar and Adigrat University for ethical clearance and financial support. The authors would also like to thank University of Gondar Comprehensive Specialized Hospital ANC staff and study participants. Finally, we would like to thank Dr Heather Dipple from England who helped us to review the manuscript for language and grammar.
Contributors The study was conceived by GMT, with additional technical guidance provided by NYM and MSB. All authors contributed to the design and data collection process, analysis and documentation of the results. GMT is acting as a guarantor for this article. All authors commented on the manuscript and approved the final draft.
Funding The authors had no a specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
Competing interests None declared.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Provenance and peer review Not commissioned; externally peer reviewed.